Part D uses the data from the subjective and objective clinical information documented within my patient visit notes (i.e., 10-years of data for 1000 patients) to revise and validate graphic displays, supplemented by explanations, to specifically answer the crucial questions asked by most patients and families about their journeys at near-end-of-life, “How long do I have to live?”, “What will the process of dying be like?”, and “Why will no one tell us how it will happen?”
